Atlas FDA

Low-Profile Visualized Intraluminal Support (LVIS) and LVIS Jr.

FDA premarket approval P170013/S006 · decided 2021-07-16

Approval details

PMA number
P170013
Supplement
S006
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Low-Profile Visualized Intraluminal Support (LVIS) and LVIS Jr.
Generic name
Intracranial coil-assist stent
Applicant
MicroVention, Inc.
Date received
2021-04-23
Decision date
2021-07-16
Days to decision
84 days
Decision code
APPR
Product code
QCA
Advisory committee
Neurology
Expedited review
No
Location
Aliso Viejo, CA
Statement
Approval for the change in antioxidants used in the dispenser hoop of packaging of the Flow Re-Direction Endoluminal Device (FRED) System, Woven EndoBridge (WEB) Aneurysm Embolization System and Low-Profile Visualized Intraluminal Support (LVIS) and LVIS Jr. devices.

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510(k) clearances by this applicant

RecordFirmDate
Wedge XL Delivery Catheter (K232542)MicroVention, Inc.2024-05-16
SOFIA EX Intracranial Support Catheter (K230775)MicroVention, Inc.2023-09-14
EmPro EPS (EP4514C-190, EP6514C-190);Nanoparasol EPS (PNP4514C-190,PNP6514C-190) (K222694)MicroVention, Inc.2023-04-27
ISAAC Neurovascular Navigation Catheter (K222115)MicroVention, Inc.2023-01-10
AZUR HydroPack 18 (45-880005; 45-880010; 45-880020; 45-880035; 45-880050; 45-880060) (K223050)MicroVention, Inc.2022-12-21
SOFIA 88 Catheter (K214024)MicroVention, Inc.2022-09-12
ERIC Retrieval Device (K211120)MicroVention, Inc.2022-03-31
BOBBY Balloon Guide Catheter (K193607)MicroVention, Inc.2020-07-21